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2,655 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
8 matches for
Jurgens SJ.
Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots
Agrawal S,
Wang M,
Klarqvist MDR,
Smith K,
Shin J,
Dashti H,
Diamant N,
Choi SH,
Jurgens SJ,
Ellinor PT,
Philippakis A,
Claussnitzer M
and 4 more — show all
Nature communications · 2022 · PMID 35773277 · open access
12 pages+
The Genetic Determinants of Aortic Distention
Pirruccello JP,
Rämö JT,
Choi SH,
Chaffin MD,
Kany S,
Nekoui M,
Chou EL,
Jurgens SJ,
Friedman SF,
Juric D,
Stone JR,
Batra P
and 4 more — show all
Journal of the American College of Cardiology · 2023 · PMID 37019578
12 pages+
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
Tadros R,
Zheng SL,
Grace C,
Jordà P,
Francis C,
West DM,
Jurgens SJ,
Thomson KL,
Harper AR,
Ormondroyd E,
Xu X,
Theotokis PI
and 50 more — show all
Buchan RJ,
McGurk KA,
Mazzarotto F,
Boschi B,
Pelo E,
Lee M,
Noseda M,
Varnava A,
Vermeer AMC,
Walsh R,
Amin AS,
van Slegtenhorst MA,
Roslin NM,
Strug LJ,
Salvi E,
Lanzani C,
de Marvao A,
Roberts JD,
Tremblay-Gravel M,
Giraldeau G,
Cadrin-Tourigny J,
L'Allier PL,
Garceau P,
Talajic M,
Gagliano Taliun SA,
Pinto YM,
Rakowski H,
Pantazis A,
Bai W,
Baksi J,
Halliday BP,
Prasad SK,
Barton PJR,
O'Regan DP,
Cook SA,
de Boer RA,
Christiaans I,
Michels M,
Kramer CM,
Ho CY,
Neubauer S,
Matthews PM,
Wilde AAM,
Tardif JC,
Olivotto I,
Adler A,
Goel A,
Ware JS,
Bezzina CR,
Watkins H
Hypergenes InterOmics Collaborators · HCMR Investigators
Nature genetics · 2025 · PMID 39966646 · open access
12 pages+
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Roselli C,
Surakka I,
Olesen MS,
Sveinbjornsson G,
Marston NA,
Choi SH,
Holm H,
Chaffin M,
Gudbjartsson D,
Hill MC,
Aegisdottir H,
Albert CM
and 145 more — show all
Alonso A,
Anderson CD,
Arking DE,
Arnar DO,
Barnard J,
Benjamin EJ,
Braunwald E,
Brumpton B,
Campbell A,
Chami N,
Chasman DI,
Cho K,
Choi EK,
Christophersen IE,
Chung MK,
Conen D,
Crijns HJ,
Cutler MJ,
Czuba T,
Damrauer SM,
Dichgans M,
Dörr M,
Dudink E,
Duong T,
Erikstrup C,
Esko T,
Fatkin D,
Faul JD,
Ferreira M,
Freitag DF,
Ganesh SK,
Gaziano JM,
Geelhoed B,
Ghouse J,
Gieger C,
Giulianini F,
Graham SE,
Gudnason V,
Guo X,
Haggerty C,
Hayward C,
Heckbert SR,
Hveem K,
Ito K,
Johnson R,
Jukema JW,
Jurgens SJ,
Kääb S,
Kane JP,
Kany S,
Kardia SLR,
Kavousi M,
Khurshid S,
Kamanu FK,
Kirchhof P,
Kleber ME,
Knight S,
Komuro I,
Krieger JE,
Launer LJ,
Li D,
Lin H,
Lin HJ,
Loos RJF,
Lotta L,
Lubitz SA,
Lunetta KL,
Macfarlane PW,
Magnusson PKE,
Malik R,
Mantineo H,
Marcus GM,
März W,
McManus DD,
Melander O,
Melloni GEM,
Meyre PB,
Miyazawa K,
Mohanty S,
Monfort LM,
Müller-Nurasyid M,
Nafissi NA,
Natale A,
Nazarian S,
Ostrowski SR,
Pak HN,
Pang S,
Pedersen OB,
Pedersen NL,
Pereira AC,
Pirruccello JP,
Preuss M,
Psaty BM,
Pullinger CR,
Rader DJ,
Rämö JT,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rotter JI,
Sabatine MS,
Schunkert H,
Shah SH,
Shim J,
Shoemaker MB,
Simonson B,
Sinner MF,
Smit RAJ,
Smith JA,
Smith NL,
Smith JG,
Soliman EZ,
Sørensen E,
Sotoodehnia N,
Strbian D,
Stricker BH,
Teder-Laving M,
Sun YV,
Thériault S,
Thorolfsdottir RB,
Thorsteinsdottir U,
Tveit A,
van der Harst P,
van Meurs J,
Wang B,
Weiss S,
Wells QS,
Weng LC,
Wilson PW,
Xiao L,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Zhao W,
Zhao W,
Zhou X,
Zöllner S,
Ruff CT,
Bundgaard H,
Willer C,
Stefansson K,
Ellinor PT
BioBank Japan Project · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2025 · PMID 40050429
12 pages+
Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk
Kany S,
Rämö JT,
Hou C,
Jurgens SJ,
Khurshid S,
Nauffal V,
Cunningham JW,
Lau ES,
Koyama S,
Ho JE,
Olgin JE,
Elmariah S
and 4 more — show all
FinnGen
Nature genetics · 2026 · PMID 41419685 · open access
12 pages+
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Barc J,
Tadros R,
Glinge C,
Chiang DY,
Jouni M,
Simonet F,
Jurgens SJ,
Baudic M,
Nicastro M,
Potet F,
Offerhaus JA,
Walsh R
and 134 more — show all
Choi SH,
Verkerk AO,
Mizusawa Y,
Anys S,
Minois D,
Arnaud M,
Duchateau J,
Wijeyeratne YD,
Muir A,
Papadakis M,
Castelletti S,
Torchio M,
Ortuño CG,
Lacunza J,
Giachino DF,
Cerrato N,
Martins RP,
Campuzano O,
Van Dooren S,
Thollet A,
Kyndt F,
Mazzanti A,
Clémenty N,
Bisson A,
Corveleyn A,
Stallmeyer B,
Dittmann S,
Saenen J,
Noël A,
Honarbakhsh S,
Rudic B,
Marzak H,
Rowe MK,
Federspiel C,
Le Page S,
Placide L,
Milhem A,
Barajas-Martinez H,
Beckmann BM,
Krapels IP,
Steinfurt J,
Winkel BG,
Jabbari R,
Shoemaker MB,
Boukens BJ,
Škorić-Milosavljević D,
Bikker H,
Manevy F,
Lichtner P,
Ribasés M,
Meitinger T,
Müller-Nurasyid M,
Veldink JH,
van den Berg LH,
Van Damme P,
Cusi D,
Lanzani C,
Rigade S,
Charpentier E,
Baron E,
Bonnaud S,
Lecointe S,
Donnart A,
Le Marec H,
Chatel S,
Karakachoff M,
Bézieau S,
London B,
Tfelt-Hansen J,
Roden D,
Odening KE,
Cerrone M,
Chinitz LA,
Volders PG,
van de Berg MP,
Laurent G,
Faivre L,
Antzelevitch C,
Kääb S,
Arnaout AA,
Dupuis JM,
Pasquie JL,
Billon O,
Roberts JD,
Jesel L,
Borggrefe M,
Lambiase PD,
Mansourati J,
Loeys B,
Leenhardt A,
Guicheney P,
Maury P,
Schulze-Bahr E,
Robyns T,
Breckpot J,
Babuty D,
Priori SG,
Napolitano C,
de Asmundis C,
Brugada P,
Brugada R,
Arbelo E,
Brugada J,
Mabo P,
Behar N,
Giustetto C,
Molina MS,
Gimeno JR,
Hasdemir C,
Schwartz PJ,
Crotti L,
McKeown PP,
Sharma S,
Behr ER,
Haissaguerre M,
Sacher F,
Rooryck C,
Tan HL,
Remme CA,
Postema PG,
Delmar M,
Ellinor PT,
Lubitz SA,
Gourraud JB,
Tanck MW,
George AL Jr,
MacRae CA,
Burridge PW,
Dina C,
Probst V,
Wilde AA,
Schott JJ,
Redon R,
Bezzina CR
KORA-Study Group · Nantes Referral Center for inherited cardiac arrhythmia
Nature genetics · 2022 · PMID 35210625
5 pages
Deep learning of left atrial structure and function provides link to atrial fibrillation risk
Pirruccello JP,
Di Achille P,
Choi SH,
Rämö JT,
Khurshid S,
Nekoui M,
Jurgens SJ,
Nauffal V,
Kany S,
Ng K,
Friedman SF,
Batra P
and 6 more — show all
FinnGen
Nature communications · 2024 · PMID 38773065 · open access
4 pages
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
Jurgens SJ,
Rämö JT,
Kramarenko DR,
Wijdeveld LFJM,
Haas J,
Chaffin MD,
Garnier S,
Gaziano L,
Weng LC,
Lipov A,
Zheng SL,
Henry A
and 46 more — show all
Huffman JE,
Challa S,
Rühle F,
Verdugo CD,
Krijger Juárez C,
Kany S,
van Orsouw CA,
Biddinger K,
Poel E,
Elliott AL,
Wang X,
Francis C,
Ruan R,
Koyama S,
Beekman L,
Zimmerman DS,
Deleuze JF,
Villard E,
Trégouët DA,
Isnard R,
Boomsma DI,
de Geus EJC,
Tadros R,
Pinto YM,
Wilde AAM,
Hottenga JJ,
Sinisalo J,
Niiranen T,
Walsh R,
Schmidt AF,
Choi SH,
Chang KM,
Tsao PS,
Matthews PM,
Ware JS,
Lumbers RT,
van der Crabben S,
Laukkanen J,
Palotie A,
Amin AS,
Charron P,
Meder B,
Ellinor PT,
Daly M,
Aragam KG,
Bezzina CR
FinnGen · VA Million Veteran Program and 1 more consortia
Nature genetics · 2024 · PMID 39572784 · open access
3 pages
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.